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Den Hollander, Anneke I., Corominas, Jordi, Colijn, Johanna Maria, Geerlings, Maartje 
ORCID: 0000-0003-1164-3573, Fauser, Sascha, de Jong, Eiko, van Duijn, Cornelia, Hoyng, Carel C. B. and Klaver, Caroline C. W.
(2018).
Whole-exome sequencing in age-related macular degeneration identifies rare protein-altering variants in COL8A1, a component of Bruch's membrane.
Invest. Ophthalmol. Vis. Sci., 59 (9).
ROCKVILLE:
ASSOC RESEARCH VISION OPHTHALMOLOGY INC.
ISSN 1552-5783
Kremlitzka, Mariann, de Jong, Sarah, Geerlings, Maartje ORCID: 0000-0003-1164-3573, Bakker, Bjorn, Nilsson, Sara C., Fauser, Sascha, Hoyng, Carel B., de Jong, Eiko K., den Hollander, Anneke I. and Blom, Anna M.
(2017).
Functional analysis of AMD-associated rare genetic variants in C9.
Mol. Immunol., 89.
S. 150 - 151.
OXFORD:
PERGAMON-ELSEVIER SCIENCE LTD.
ISSN 0161-5890
de Motta, Laura Lores, Paun, Constantin, Corominas, Jordi, Geerlings, Maartje ORCID: 0000-0003-1164-3573, Altay, Lebriz, Schick, Tina, Bakker, Bjorn, Groenewoud, Joannes, Daha, Mohamed, Fauser, Sascha, Den Hollander, Anneke I. and de Jong, Eiko
(2017).
Towards precision medicine in AMD: Genome-wide association study reveals genetic variants in CFH and CFHR4 that are strongly associated with complement activation levels.
Invest. Ophthalmol. Vis. Sci., 58 (8).
ROCKVILLE:
ASSOC RESEARCH VISION OPHTHALMOLOGY INC.
ISSN 1552-5783
Geerlings, Maartje ORCID: 0000-0003-1164-3573, Saksens, Nicole T. M., Bakker, Bjorn, Schick, Tina, Fauser, Sascha, Boon, Camiel J. F., de Jong, Eiko, Hoyng, Carel C. B. and Den Hollander, Anneke I.
(2015).
Rare variants in complement genes associated with age-related macular degeneration result in a lower age at onset and higher familial occurrence.
Invest. Ophthalmol. Vis. Sci., 56 (7).
ROCKVILLE:
ASSOC RESEARCH VISION OPHTHALMOLOGY INC.
ISSN 1552-5783